1. Home
  2. Labeler Index
  3. Three Kings Corp
  4. NDC Product Code: 72898-001 Dab

NDC 72898-001 Dab

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72898-001?
  4. Dab Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
72898-001
Proprietary Name:
Dab
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Three Kings Corp
Labeler Code:
72898
Product Label ID:
9e42c2fb-0499-53ad-e053-2995a90a923c
Start Marketing Date: [9]
02-10-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72898-001-01

Package Description: 45 mL in 1 BOTTLE, PUMP

NDC Code 72898-001-02

Package Description: 250 mL in 1 BOTTLE, PUMP

NDC Code 72898-001-03

Package Description: 1200 mL in 1 BOTTLE, PUMP

NDC Code 72898-001-04

Package Description: 946352 mL in 1 DRUM

Product Details

What is NDC 72898-001?

The NDC code 72898-001 is assigned by the FDA to the product Dab which is product labeled by Three Kings Corp. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 72898-001-01 45 ml in 1 bottle, pump , 72898-001-02 250 ml in 1 bottle, pump , 72898-001-03 1200 ml in 1 bottle, pump , 72898-001-04 946352 ml in 1 drum . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Dab?

Receive a small amount of foam into palm of handrub thoroughly over all surfaces of both handsrub hands together until dry

Which are Dab UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Dab Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Dab?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".